Canonical Allele Identifier: CA491478127
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1215485605

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322700G>A , CM000677.2:g.73322700G>A GRCh38
NC_000015.9:g.73615041G>A , CM000677.1:g.73615041G>A GRCh37
NC_000015.8:g.71402094G>A NCBI36
NG_009063.1:g.51565C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3393C>T MANE Select ENSP00000261917.3:p.Ser1131=
ENST00000261917.3:c.3393C>T ENSP00000261917.3:p.Ser1131=
NM_005477.2:c.3393C>T NP_005468.1:p.Ser1131=
XM_011521148.1:c.2175C>T XP_011519450.1:p.Ser725=
XM_011521148.2:c.2175C>T XP_011519450.1:p.Ser725=
NM_005477.3:c.3393C>T MANE Select NP_005468.1:p.Ser1131=